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PubChem

Soybean Oil

PubChem Reference Collection SID
PubChem CID
Not available and might not be a discrete structure.
Description
Oils, edible: soya bean is a pale yellow oily liquid with a weak odor. Floats on water. Contains principally glycerides of oleic and linoleic acids.
Derived from soybeans, soybean oil is a common vegetable oil and a source of polyunsaturated and saturated fatty acids. It is a complex mixture of triglycerides where per 100 g, soybean oil has 16 g of saturated fat, 23 g of monounsaturated fat, and 58 g of polyunsaturated fat. The major component fatty acids are linoleic (48% - 58%), oleic (17% - 30%), palmitic (9% -13%), linolenic (4% - 11%), and stearic (2.5% - 5.0%). It is used as a cooking oil and lipid emulsion for parenteral nutrition in clinical settings. Soybean oil-based lipid emulsion is the only FDA-approved lipid formulation for clinical use.
Soybean oil is a Lipid Emulsion.
See also: Olive Oil (related); Coconut Oil (related); Safflower Oil (related) ... View More ...

1 Synonyms

  • Soybean Oil
  • CHEBI:166975
  • CIPHERKEY HAIR TONIC
  • CIPHERKEYshampoo
  • DTXSID8027660
  • ENDOLIPIDE COMPONENT SOYA OIL
  • Glycine Soja (Soybean) Oil
  • I. V. Fat Emulsion
  • I.V. Fat Emulsion
  • Intralipid (fresenius)
  • JANGBALZZANG BIOTINshampoo
  • JANGBALZZANG HAIR TONIC
  • Liposyn (hospira)
  • NutriLipid I.V. Fat Emulsion
  • Nutrilipid
  • Nutrilipid (b braun)
  • Oil, Soy Bean
  • Oil, Soya
  • Oil, Soybean
  • Oils, Soy Bean
  • Oils, Soya
  • RefChem:24219
  • Soy Bean Oil
  • Soy Bean Oils
  • Soy oil
  • Soy-bean oil
  • Soya Oils
  • Soybean Oils
  • black soybean extracts
  • 232-274-4
  • 241ATL177A
  • 8001-22-7
  • Glycine max seed oil
  • Intralipid 10%
  • Intralipid 20%
  • Intralipid 30%
  • Liposyn III 10%
  • Liposyn III 20%
  • Liposyn III 30%
  • NSC406244
  • Nutrilipid 10%
  • Nutrilipid 20%
  • Oils, Soybean
  • Soya Oil
  • Soyacal 10%
  • Soyacal 20%
  • Travamulsion 10%
  • Travamulsion 20%
  • Extract of soy
  • Soybean oil, refined
  • Acidulated soybean soapstock
  • Bionatrol
  • Crude soybean oil, solvent extracted
  • Degummed soybean oil
  • Lipovenoes
  • Lipovenos
  • Lipovenous
  • Refined soybean oil
  • Refined undeodorized soybean oil
  • Soy germ extract
  • Soya-bean oil
  • Soybean acidulated soapstock
  • Soybean deodorizer distillate
  • Soybean oil bleaching
  • Soybean oil deodorization
  • Soybean oil fatty acids, glycerol triester
  • Soybean oil, bleached
  • Soybean oil, degummed
  • Soybean oil, deodorized
  • Soybean vegetable oil, winter fraction
  • VT 18

2 MeSH Entry Terms

  • Soybean Oil
  • Soy Bean Oil
  • Soya Oil

3 Names and Identifiers

3.1 Other Identifiers

3.1.1 CAS

8001-22-7

3.1.2 Deprecated CAS

152059-96-6, 358980-39-9, 8030-22-6, 84776-91-0
152059-96-6, 358980-39-9, 8030-22-6

3.1.3 European Community (EC) Number

3.1.4 UNII

3.1.5 DrugBank ID

3.1.6 DSSTox Substance ID

3.1.7 NCI Thesaurus Code

3.1.8 Nikkaji Number

3.1.9 NSC Number

3.1.10 RXCUI

4 Chemical and Physical Properties

4.1 Experimental Properties

4.1.1 Physical Description

Oils, edible: soya bean is a pale yellow oily liquid with a weak odor. Floats on water. Contains principally glycerides of oleic and linoleic acids.
Liquid, Other Solid; Water or Solvent Wet Solid; Dry Powder; Liquid; NKRA
Pale yellow oily liquid with a faint odor; [CAMEO] Clear light yellow liquid; [Sigma-Aldrich MSDS]

4.1.2 Color / Form

Pale yellow to brownish-yellow oil
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616

4.1.3 Odor

Slight characteristic odor
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616

4.1.4 Taste

Bland flavor /refined soybean oil/
Thomas A; Fats and Fatty Oils. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: June 15, 2001.

4.1.5 Boiling Point

620-650 K (347-377 °C) /primary triglyceride esters in soybean oil/
Yuan E et al; Fuel 84: 943-950 (2005)
Very high (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

4.1.6 Melting Point

Melts at 22-31 °C; Solidifies at -10 to 16 °C
Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 15th Edition. John Wiley & Sons, Inc. New York, NY 2007., p. 1166
-4 °F (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

4.1.7 Flash Point

540 °F (282 °C) closed cup
National Fire Protection Association; Fire Protection Guide to Hazardous Materials. 14TH Edition, Quincy, MA 2010, p. 325-104
540 °F (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

4.1.8 Solubility

Solubility of water in soybean oil = 0.11% by weight at 22 °C, 0.19% by weight at 60 °C
Hammond EG et al; Soybean Oil. In: Bailey's Industrial Oil and Fat Products, Sixth Ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf
Insoluble in water
NOAA; Cameo Chemicals. Oils, Edible: Soya Bean (CAS 8001-22-7), Nat Oceanic Atmos Admin. Available from, as of April 25, 2014: https://cameochemicals.noaa.gov/chemical/18016
Miscible with absolute alcohol, ether, petroleum ether, chloroform, carbon disulfide
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616

4.1.9 Density

0.916-0.922 at 25/25 °C
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616
0.922 at 68 °F (USCG, 1999) - Less dense than water; will float
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

4.1.10 Vapor Pressure

8.0X10-5 mm Hg at 25 °C /extrapolated, representative triglycerides of soybean oil/
Yuan E et al; Fuel 84: 943-950 (2005)
5.17 mmHg (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

4.1.11 Stability / Shelf Life

Stable under recommended storage conditions.
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html

4.1.12 Autoignition Temperature

833 °F (445 °C)
National Fire Protection Association; Fire Protection Guide to Hazardous Materials. 14TH Edition, Quincy, MA 2010, p. 325-104
833 °F (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

4.1.13 Viscosity

172.9 cP at 0 °C; 99.7 cP at at 10 °C; 50.09 cP at 25 °C; 28.86 cP at 40 °C
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616

4.1.14 Heat of Combustion

9135-9450 cal/g
Hammond EG et al; Soybean Oil, In: Bailey's Industrial Oil and Fat Products, Sixth Ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf

4.1.15 Heat of Vaporization

44,200 cal/mol
Hammond EG et al; Soybean Oil, In: Bailey's Industrial Oil and Fat Products, Sixth Ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf

4.1.16 Surface Tension

27.6 dyne/cm at 30 °C
Hammond EG et al; Soybean Oil, In: Bailey's Industrial Oil and Fat Products, Sixth Ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf

4.1.17 Refractive Index

Index of refraction: 1.471-1.475 at 25 °C
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616

4.1.18 Other Experimental Properties

Acid value: 0.3-3; Saponification value: 189-195; Iodine value: 127-138; Thiocyanogen value: 77-85; Hydroxyl value: 4-8; Reichert-Meissl value: 0.2-0.7; Polenske value: 0.2-1.0; Diene no. 0.7
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616
Reacts with acids to liberate heat. Heat is also generated by interaction with caustic solutions. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Flammable hydrogen is generated by mixing with alkali metals and hydrides. React slowly with oxygen in the air to become rancid.
NOAA; Cameo Chemicals. Oils, Edible: Soya Bean (CAS 8001-22-7), Nat Oceanic Atmos Admin. Available from, as of April 25, 2014: https://cameochemicals.noaa.gov/chemical/18016

4.2 Chemical Classes

Biological Agents -> Plant Oils and Extracts

4.2.1 Drugs

4.2.1.1 Human Drugs
Human drug -> Discontinued
Human drug -> Prescription
Human drug -> Active ingredient (SOYBEAN OIL)

4.2.2 Cosmetics

Cosmetic ingredients (Glycine Soja (Soybean) Oil) -> CIR (Cosmetic Ingredient Review)
International Journal of Toxicology 36(Suppl. 3):51-129, 2017

4.2.3 Food Contact Substances

FCS -> FDA Inventory of Food Contact Substances Listed in 21 CFR

4.2.4 Fragrances

Fragrance Ingredient (Refined soybean oil extract) -> IFRA transparency List
Fragrance Ingredient (Refined soybean oil extract (post treated)) -> IFRA transparency List
Fragrance Ingredient (Soybean oil, fixed) -> IFRA transparency List

4.2.5 UVCB

UVCB -> EPA TSCA

6 Drug and Medication Information

6.1 Drug Indication

In a clinical context, soybean oil is used as a source of calories and fatty acids in patients requiring parenteral nutrition. A formulation called Clinolipid, comprising soybean oil and [olive oil], is indicated in all age groups, including term and preterm neonates, as a source of calories and essential fatty acids for parenteral nutrition (PN) when oral or enteral nutrition is not possible, insufficient, or contraindicated.

6.2 FDA Approved Drugs

6.3 FDA Orange Book

6.4 FDA National Drug Code Directory

6.5 Drug Labels

Drug and label

6.6 Therapeutic Uses

Caloric/fatty acid source: Source of calories and essential fatty acids for patients requiring parenteral nutrition for extended periods of time (usually for longer than 5 days). Source of essential fatty acids when a deficiency occurs.
Drug Facts and Comparisons 2013. Wolters Kluwer Health St. Louis, MO 2013, p. 165

7 Food Additives and Ingredients

7.1 FDA Food Contact Substances (FCS)

1 of 2 items
Substance
SOYBEAN OIL
Document Number (21 eCFR)
2 of 2 items
Substance
SOYBEAN OIL, REFINED
Document Number (21 eCFR)

8 Pharmacology and Biochemistry

8.1 Pharmacodynamics

Soybean oil is a nutrition source that provides a biologically utilizable source of calories and essential fatty acids. It prevents the biochemical lesions of essential fatty acid deficiency (EFAD), and correct the clinical manifestations of the EFAD syndrome by supplying energy and nutrients.

8.2 FDA Pharmacological Classification

1 of 4 items
FDA UNII
241ATL177A
Active Moiety
SOYBEAN OIL
Pharmacological Classes
Established Pharmacologic Class [EPC] - Lipid Emulsion
Pharmacological Classes
Chemical Structure [CS] - Lipids
FDA Pharmacology Summary
Soybean oil is a Lipid Emulsion.
2 of 4 items
Non-Proprietary Name
I. V. FAT EMULSION
Pharmacological Classes
Lipid Emulsion [EPC]; Lipids [CS]
3 of 4 items
Non-Proprietary Name
I.V. FAT EMULSION
Pharmacological Classes
Lipid Emulsion [EPC]; Lipids [CS]
4 of 4 items
Non-Proprietary Name
SOYBEAN OIL
Pharmacological Classes
Lipids [CS]; Lipid Emulsion [EPC]

8.3 Absorption, Distribution and Excretion

Absorption
Following infusion, there is a transient increase in plasma triglycerides.
Route of Elimination
Converted carbon dioxide from smaller fatty acid units are excreted by the lungs.
Volume of Distribution
After triglycerides are hydrolyzed, fatty acids can enter the tissues where they may be oxidized or resynthesized into triglcerides and stored.
Clearance
The elimination rate of lipid emulsions depends on particle size, fatty acid composition, apolipoprotein content of the lipid globules, lipoprotein lipase activity, and hepatic lipase activity.

8.4 Metabolism / Metabolites

The infused lipid particles are removed from the bloodstream in a manner generally thought to be similar to the enzymatic clearance of naturally produced chylomicrons formed after enteral fat intake. The triglycerides are hydrolyzed to free fatty acids and glycerol by the enzyme lipoprotein lipase. In the liver, circulating free fatty acids are oxidized or converted to very low density lipoproteins by hepatic lipase that re-enter the bloodstream.

8.5 Mechanism of Action

Fatty acids serve as an important substrate for energy production. The most common mechanism of action for energy production derived from fatty acid metabolism is beta oxidation. Fatty acids are also important for membrane structure and function, precursors for bioactive molecules (such as prostaglandins), and as regulators of gene expression. Soybean oil-based lipid emulsion may also cause an increase in heat production, decrease in respiratory quotient, and increase in oxygen consumption following its administration. Soybean oil contents prevent abnormally high triacylglycerol synthesis and its accumulation as lipid droplets in the liver by regulating hepatic lipogenesis and lipolysis. In vitro, soybean oil is shown to prevent downregulation of CYP2C2, CYP2C11 and CYP3A2 mRNA thus maintaining hepatic drug oxidation capabilities. Soybean oil is broken down into free fatty acids that activate PPAR-alpha, which regulate hepatic CYP4A1 that hydroxylate saturated and unsaturated fatty acids. Soybean oil is also shown to prevent up/downregulation of efflux transporters and maintain mRNA levels of hepatic antioxidant enzymes in vitro rat studies.

9 Use and Manufacturing

9.1 Uses

For soybean oil (USEPA/OPP Pesticide Code: 031605) ACTIVE products with label matches. /SRP: Registered for use in the USA but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./
National Pesticide Information Retrieval System's Database on Soybean OIl (8001-22-7). Available from, as of July 11, 2014: https://npirspublic.ceris.purdue.edu/ppis/
Herbicide, insecticide.
Crop Protection Handbook Volume 100, Meister Media Worldwide, Willoughby, OH 2014, p. 538
As a cooking and salad oil. In the manufacture of margarine, shortenings, mayonnaise, candy, soap. In paints, varnishes, resins, plastics, and biodiesel fuel.
O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1616
Soap manufacture, high-protein foods, paints and varnishes, cattle feeds, margarine and salad dressings, printing inks, source of nylon9, plasticizers (epoxidized), alkyd resins
Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 15th Edition. John Wiley & Sons, Inc. New York, NY 2007., p. 1166
For more Uses (Complete) data for Soybean oil (9 total), please visit the HSDB record page.
Cosmetic Ingredient Review Link
International Journal of Toxicology 36(Suppl. 3):51-129, 2017
Sources/Uses
Used as an insecticide/miticide for use on citrus fruits, various ornamentals, domestic dwellings and premises, and recreational areas; [Reference #1] Permitted for use as an inert ingredient in non-food pesticide products; [EPA]
Industrial Processes with risk of exposure
Farming (Pesticides) [Category: Industry]

9.1.1 Use Classification

EPA Safer Chemical Functional Use Classes -> Processing Aids and Additives
Safer Chemical Classes -> Green circle Green circle - The chemical has been verified to be of low concern
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Fragrance Ingredients

9.1.2 Industry Uses

  • Surface active agents
  • Flotation agent
  • Paint additives and coating additives not described by other categories
  • Dust suppressant
  • Solvent
  • Not Known or Reasonably Ascertainable
  • Intermediates
  • Other (specify)
  • Defoamer

9.1.3 Consumer Uses

Paint additives and coating additives not described by other categories

9.1.4 Household Products

Household & Commercial/Institutional Products

Information on 142 consumer products that contain Soybean oil blend in the following categories is provided:

• Auto Products

• Commercial / Institutional

• Home Maintenance

• Inside the Home

• Landscaping/Yard

• Personal Care

• Pesticides

• Pet Care

9.2 Methods of Manufacturing

Soybeans are normally cracked and flaked prior to extraction with hexane. Preexpelling is not normally performed. ... Soybean oil is often postdegummed with phosphoric or citric acid prior to neutralization with lye, earth bleaching, and deodorization.
Thomas A; Fats and Fatty Oils. Ullmann's Encyclopedia of Industrial Chemistry 7th ed. (1999-2014). NY, NY: John Wiley & Sons. Online Posting Date: June 15, 2000
From the seed of the legume Glycine max. /Soybean oil (unhydrogenated)/
Lewis, R.J. Sr. (ed) Sax's Dangerous Properties of Industrial Materials. 11th Edition. Wiley-Interscience, Wiley & Sons, Inc. Hoboken, NJ. 2004., p. 3293

9.3 Formulations / Preparations

Emulsifiable concentrate.
USEPA/Office of Prevention, Pesticides and Toxic Substances; Reregistration Eligibility Decision Document - Flower and Vegetable Oils p.8 EPA 738-R-93-031 (December 1993). Available from, as of July 14, 2014: https://www.epa.gov/oppsrrd1/REDs/old_reds/flower_veggie_oils.pdf
Premix Partners: Corn gluten meal.
Crop Protection Handbook Volume 100, Meister Media Worldwide, Willoughby, OH 2014, p. 538
GWN-9996 (Gowan Company): Active ingredient: soybean oil 59.3%, resins, oleo-, capsicum 7.6%, and garlic oil 23.4%.
National Pesticide Information Retrieval System's Database on Soybean Oil (8001-22-7). Available from, as of July 11, 2014: https://npirspublic.ceris.purdue.edu/ppis/
Citru-Soy (Drexel Chemical Company): Active ingredient: soybean oil 98.0%.
National Pesticide Information Retrieval System's Database on Soybean Oil (8001-22-7). Available from, as of July 11, 2014: https://npirspublic.ceris.purdue.edu/ppis/
For more Formulations/Preparations (Complete) data for Soybean oil (15 total), please visit the HSDB record page.

9.4 Consumption Patterns

The use of inks produced from soybean oil in the US increased by fourfold between 1989 and 2000 and is now at more than 22% of total use.
Curran MA; Biobased Materials. Kirk-Othmer Encyclopedia of Chemical Technology. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: March 12, 2010.

9.5 U.S. Production

Soybean oil is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).
EPA/Office of Pollution Prevention and Toxics; High Production Volume (HPV) Challenge Program. Soybean Oil (8001-22-7). Available from, as of July 10, 2014: https://www.epa.gov/hpv/pubs/general/opptsrch.htm
Production volumes for non-confidential chemicals reported under the Inventory Update Rule.
Year
1986
Production Range (pounds)
>1 billion
Year
1990
Production Range (pounds)
>1 billion
Year
1994
Production Range (pounds)
>1 billion
Year
1998
Production Range (pounds)
>1 billion
Year
2002
Production Range (pounds)
>1 billion
US EPA; Non-confidential Production Volume Information Submitted by Companies for Chemicals Under the 1986-2002 Inventory Update Rule (IUR). Soybean Oil (8001-22-7). Available from, as of July 10, 2014: https://epa.gov/cdr/tools/data/2002-vol.html
Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: Soybean oil. Aggregated National Production Volume: 1 billion pounds and greater.
US EPA; Non-Confidential 2006 Inventory Update Reporting. National Chemical Information. Soybean Oil (8001-22-7). Available from, as of July 11, 2014: https://cfpub.epa.gov/iursearch/index.cfm
Non-confidential 2014 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Soybean oil. National Production Volume: 3,183,346,050 lb/yr.
USEPA/Pollution Prevention and Toxics; 2014 Chemical Data Reporting Database. Soybean Oil (8001-22-7). Available from, as of July 11, 2014: https://java.epa.gov/oppt_chemical_search/
Aggregated Product Volume

2019: 5,000,000,000 - <10,000,000,000 lb

2018: 5,000,000,000 - <10,000,000,000 lb

2017: 5,000,000,000 - <10,000,000,000 lb

2016: 5,000,000,000 - <10,000,000,000 lb

9.6 General Manufacturing Information

Processed soybeans are the world's largest source of animal protein feed and the second largest source of vegetable oil. The United States is the leading soybean producer and exporter. Soybeans comprise about 90 percent of U.S. oilseed production, while other oilseeds--including peanuts, sunflowerseed, canola, and flax--make up the remainder.
United States Department of Agriculture; Economic Research Service; Soybeans & Oil Crops; Available from, as of May 19, 2014: https://ers.usda.gov/topics/crops/soybeans-oil-crops.aspx#.U1VcfVVdXZc
Soybean oil is a complex mixture of five fatty acids (palmitic, stearic, oleic, linoleic, and linolenic acids) that have vastly differing melting points, oxidative stabilities, and chemical functionalities.
Cahoon EB; AgBioForum 6 (1&2): 11-13 (2003)
Industry Processing Sectors
  • Not Known or Reasonably Ascertainable
  • Plastics Material and Resin Manufacturing
  • All Other Chemical Product and Preparation Manufacturing
  • Printing and Related Support Activities
  • Paper Manufacturing
  • Plastics Product Manufacturing
  • Adhesive Manufacturing
  • Paint and Coating Manufacturing
  • Food, beverage, and tobacco product manufacturing
  • Mining (except Oil and Gas) and support activities
EPA TSCA Commercial Activity Status
Soybean oil: ACTIVE

10 Safety and Hazards

10.1 Hazards Identification

10.1.1 GHS Classification

Note
This chemical does not meet GHS hazard criteria for 96.1% (1235 of 1285) of all reports.
GHS Hazard Statements

Not Classified

Reported as not meeting GHS hazard criteria by 1235 of 1285 companies (only 3.9% companies provided GHS information). For more detailed information, please visit ECHA C&L website.

ECHA C&L Notifications Summary

Aggregated GHS information provided per 1285 reports by companies from 4 notifications to the ECHA C&L Inventory.

Reported as not meeting GHS hazard criteria per 1235 of 1285 reports by companies.

There are 2 notifications provided by 50 of 1285 reports by companies with hazard statement code(s).

Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

10.1.2 Hazard Classes and Categories

Not Classified

10.1.3 NFPA Hazard Classification

NFPA 704 Diamond
0-1-0
NFPA Health Rating
0 - Materials that, under emergency conditions, would offer no hazard beyond that of ordinary combustible materials.
NFPA Fire Rating
1 - Materials that must be preheated before ignition can occur. Materials require considerable preheating, under all ambient temperature conditions, before ignition and combustion can occur.
NFPA Instability Rating
0 - Materials that in themselves are normally stable, even under fire conditions.

10.1.4 EPA Safer Chemical

Chemical: Soybean oil

Green circle Green circle - The chemical has been verified to be of low concern based on experimental and modeled data.

10.1.5 Health Hazards

None-is a food. (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

10.1.6 Hazards Summary

TSCA Definition 2008: Extractives and their physically modified derivatives. It consists primarily of the glycerides of the fatty acids linoleic, oleic, palmitic and stearic. (Soja hispida). [ChemIDplus] Generally regarded as safe (GRAS) by the FDA; [Reference #1] Not considered hazardous by GHS classification; [Sigma-Aldrich MSDS]

10.1.7 Fire Potential

Reacts with acids to liberate heat. Heat is also generated by interaction with caustic solutions. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Flammable hydrogen is generated by mixing with alkali metals and hydrides. React slowly with oxygen in the air to become rancid.
NOAA; Cameo Chemicals. Oils, Edible: Soya Bean (CAS 8001-22-7), Nat Oceanic Atmos Admin. Available from, as of April 25, 2014: https://cameochemicals.noaa.gov/chemical/18016

10.2 First Aid Measures

10.2.1 First Aid

EYES: flush with water for at least 15 min. (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

10.3 Fire Fighting

Fire Extinguishing Agents Not to Be Used: Water or foam may cause frothing.

Fire Extinguishing Agents: Dry chemical, foam, or carbon dioxide (USCG, 1999)

U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

10.3.1 Fire Fighting Procedures

Water or Foam May Cause Frothing.
National Fire Protection Association; Fire Protection Guide to Hazardous Materials. 14TH Edition, Quincy, MA 2010, p. 325-104
Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Special protective equipment for firefighters: Wear self contained breathing apparatus for fire fighting if necessary.
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html

10.4 Accidental Release Measures

10.4.1 Cleanup Methods

Environmental precautions: Do not let product enter drains. Methods and materials for containment and cleaning up: Keep in suitable, closed containers for disposal.
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html

10.4.2 Disposal Methods

SRP: Criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
Product: Offer surplus and non-recyclable solutions to a licensed disposal company. Contaminated packaging: Dispose of as unused product.
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html

10.5 Handling and Storage

10.5.1 Storage Conditions

Store at 20 deg to 25 °C (68 to 77 °F); do not freeze. /Intralipid 20%, Liposyn III 30%/
Drug Facts and Comparisons 2013. Wolters Kluwer Health St. Louis, MO 2013, p. 164
Store at 30 °C (86 °F) or below; do not freeze /Liposyn III 10%, Liposyn III 20%, Liposyn II 10%, Liposyn II 20%/
Drug Facts and Comparisons 2013. Wolters Kluwer Health St. Louis, MO 2013, p. 164
Should not be stored above 25 °C (77 °F); do not freeze. /Intralipid 30%/
Drug Facts and Comparisons 2013. Wolters Kluwer Health St. Louis, MO 2013, p. 164

10.6 Exposure Control and Personal Protection

10.6.1 Personal Protective Equipment (PPE)

Eye protection: Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html
Respiratory protection: Respiratory protection not required. For nuisance exposures use type OV/AG (US) or type ABEK (EU EN 14387) respirator cartridges. Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html
Skin and body protection: impervious clothing, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html
Hand protection: Handle with gloves.
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html
Goggles or face shield. (USCG, 1999)
U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.

10.7 Stability and Reactivity

10.7.1 Air and Water Reactions

Insoluble in water.

10.7.2 Reactive Group

Esters, Sulfate Esters, Phosphate Esters, Thiophosphate Esters, and Borate Esters

Hydrocarbons, Aliphatic Unsaturated

10.7.3 Reactivity Profile

OILS, EDIBLE: SOYA BEAN react with acids to liberate heat. Heat is also generated by interaction with caustic solutions. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Flammable hydrogen is generated by mixing with alkali metals and hydrides. React slowly with oxygen in the air to become rancid.

10.7.4 Hazardous Reactivities and Incompatibilities

Soybean oil react with acids to liberate heat. Heat is also generated by interaction with caustic solutions. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Flammable hydrogen is generated by mixing with alkali metals and hydrides. React slowly with oxygen in the air to become rancid.
Chemical Book; Soybean Oil (CAS No. 8001-22-7) (2010). Avaiable from, as of September 15, 2014: https://www.chemicalbook.com/ChemicalProductProperty_EN_CB2703220.htm
Materials to avoid: Strong oxidizing agents.
Sigma-Aldrich; Material Safety Data Sheet for Soybean oil, Product Number: S7381, Version 4.1 (Revision Date 11/21/2012). Available from, as of June 3, 2014: https://www.sigmaaldrich.com/safety-center.html

10.8 Regulatory Information

The Australian Inventory of Industrial Chemicals
Chemical: Soybean oil
New Zealand EPA Inventory of Chemical Status
Soybean oil: Does not have an individual approval but may be used under an appropriate group standard

10.8.1 FIFRA Requirements

Based on the reviews of the generic data for the active ingredients flower and vegetable oils /including soybean oil/, the Agency has sufficient information on the health effects of flower and vegetable oils and on it potential for causing adverse effects in fish and wildlife and the environment. Therefore, the Agency concludes that products containing flower and vegetable oils for all uses, except the use of essential oils in antimicrobial products, are eligible for reregistration. The Agency has determined that the flower and vegetable oils products, labeled and used as specified in this Reregistration Eligibility Decision, will not pose unreasonable risks or adverse effects to humans or the environment.
USEPA/Office of Prevention, Pesticides and Toxic Substances; Reregistration Eligibility Decision Document - Flower and Vegetable Oils p.20 EPA 738-R-93-031 (December 1993). Available from, as of July 14, 2014: https://www.epa.gov/oppsrrd1/REDs/old_reds/flower_veggie_oils.pdf
As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer saftey standards, such as those described in the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA '88 were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern than those on List C, and with List C containing pesticides of greater concern than those on List D. Soybean oil is found on List D. Case No: 4097; Pesticide type: insecticide, fungicide, herbicide, rodenticide, antimicrobial; Case Status: RED Approved 01/94; OPP has made a decision that some/all uses of the pesticide are eligible for reregistration, as reflected in a Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): soybean oil; Data Call-in (DCI) Date(s): 02/22/94; AI Status: OPP has completed a Reregistration Eligibility Decision (RED) for the case/AI.
United States Environmental Protection Agency/ Prevention, Pesticides and Toxic Substances; Status of Pesticides in Registration, Reregistration, and Special Review. (1998) EPA 738-R-98-002, p. 344

10.8.2 FDA Requirements

Substances migrating to food from cotton and cotton fabrics used in dry food packaging that are generally recognized as safe for their intended use, within the meaning of section 409 of the Act. Soybean oil (hydrogenated) is included on this list.
21 CFR 182.70 (USFDA); U.S. National Archives and Records Administration's Electronic Code of Federal Regulations. Available from, as of July 14, 2014: https://www.ecfr.gov
Polyglycerol esters of fatty acids, up to and including the decaglycerol esters, may be safely used in food in accordance with the following prescribed conditions: (a) They are prepared from corn oil, cottonseed oil, lard, palm oil from fruit, peanut oil, safflower oil, sesame oil, soybean oil, and tallow and the fatty acids derived from these substances (hydrogenated and nonhydrogenated) meeting the requirements of section 172.860(b) and/or oleic acid derived from tall oil fatty acids meeting the requirements of 172.862. (b) They are used as emulsifiers in food, in amounts not greater than that required to produce the intended physical or technical effect.
21 CFR 172.854 (USFDA); U.S. National Archives and Records Administration's Electronic Code of Federal Regulations. Available from, as of July 10, 2014: https://www.ecfr.gov

10.9 Other Safety Information

Chemical Assessment

IMAP assessments - Soybean oil: Environment tier I assessment

IMAP assessments - Soybean oil: Human health tier I assessment

10.9.1 Toxic Combustion Products

When heated to decomposition it emits acrid smoke and irritating fumes. /Soybean oil (unhydrogenated)/
Lewis, R.J. Sr. (ed) Sax's Dangerous Properties of Industrial Materials. 11th Edition. Wiley-Interscience, Wiley & Sons, Inc. Hoboken, NJ. 2004., p. 3293

10.9.2 Special Reports

USEPA/Office of Prevention, Pesticides and Toxic Substances; Reregistration Eligibility Decision Document - Flower and Vegetable Oils, EPA 738-R-93-031 (December 1993). The RED summarizes the risk assessment conclusions and outlines any risk reduction measures necessary for the pesticide to continue to be registered in the U.S.[Available from, as of July 14, 2014: http://www.epa.gov/oppsrrd1/REDs/old_reds/flower_veggie_oils.pdf]
Genetic Enhancement of Soybean Oil for Industrial Uses: Prospects and Challenges.[Cahoon EB; AgBioForum 6 (1&2): 11-13 (2003)]

11 Toxicity

11.1 Toxicological Information

11.1.1 Toxicity Summary

IDENTIFICATION AND USE: Soybean oil is a pale yellow to brownish-yellow oil with a slight characteristic odor. It is used as a cooking and salad oil, in the manufacture of margarine, shortenings, mayonnaise, and candy. It is also used in production of soap, paints, varnishes, resins, plastics, and biodiesel fuel. In medicine, soybean oil is used in parenteral nutrition formulations as a source of calories and essential fatty acids. HUMAN EXPOSURE AND TOXICITY: Soybean oil emulsion given as a single dose of 500 mL promotes lymphocyte and neutrophil death that may enhance the susceptibility of the patients to infections. Death in preterm infants after infusion of iv fat emulsions have occurred. Autopsy findings included intravascular fat accumulation in the lungs. A person who worked and lived near a soya bean mill experienced asthma which was dependent on the wind direction. He gave a positive reaction to skin scratch tests with soya bean products, including soya bean oil of unspecified grade. The genotoxicity and cytotoxicity of the oil fumes formed from heating three common commercial cooking oils (soybean oil, sunflower oil, and lard) was tested on human lung carcinoma pulmonary type II-like epithelium cell (A-549 cell). The results indicated that the methanolic extracts of oil fumes could apparently lead to cytotoxicity and oxidative DNA damage. Glutathione (GSH) contents and the activities of antioxidant enzymes were adversely reduced by the methanolic extracts of oil fumes. When human A-549 cells were exposed to the methanolic extracts of oil fumes for 30 min, there was an increase in the formation of intracellular reactive oxygen species (ROS). Moreover, the methanolic extracts of oil fumes caused significant oxidative damage through the 8-hydroxy-2'-deoxyguanosine formation in A-549 cells at the concentrations from 50 to 200 ug/mL. These results demonstrated that the DNA damage in A-549 cells, induced by cooking oil fumes, was related to the ROS formation and may have implications for lung cancer. ANIMAL STUDIES: The effect of continuous Intralipid infusions on serum HDL and LDL levels was studied in the rat. Total cholesterol, HDL-cholesterol and LDL-cholesterol levels were significantly elevated following 96 hr of infusion with 10% Intralipid with food intake significantly decreased compared to a control group. Futhermore, soybean oil-based emulsion promoted the apoptosis of splenic lymphocytes in mice. Infusion of soybean oil-based emulsions augmented the apoptosis of splenic and circulating lymphocytes in murine model of acute lung injury (ALI) and led to increased mortality in mice. These findings may be of relevance for patients experiencing ALI that require parenteral nutrition. In developmental study rats were divided into three groups according to dietary fat source: PM (40% crude palm oil), SB (40% soybean oil), and VS (40% partially hydrogenated vegetable shortening). Rats were fed experimental diets from day 1 of pregnancy to sacrifice, which was one week after weaning of pups (21 d). Milk was expressed from dams on day 14 of lactation. PM, SB and VS milk samples had the same fat content and had fatty acid profiles similar to that of their respective diets. SB and VS dams had significantly more pups dead at birth compared to PM dams. Soybean oil was tested for genotoxicity in the Drosophila wing somatic mutation and recombination assay. Results indicate that the oil produces genotoxic effects when tested without any previous frying or boiling processes.
Cosmetic Ingredient Review Finding(s)
Safe in the present practices of use and concentration. Ingredient, concentration, and use information are available in documents discoverable at https://cir-reports.cir-safety.org
International Journal of Toxicology 36(Suppl. 3):51-129, 2017

11.1.2 Acute Effects

11.1.3 Interactions

The reported successful use of IV lipid emulsions in local anesthetic intoxications is thought to be due to lipid sequestration of local anesthetics. However, controlled efficacy studies were lacking, and other mechanisms of action have also been suggested. This study investigated the effect of lipid infusion on plasma concentrations and cardiovascular effects of 2 local anesthetics differing in lipophilicity, bupivacaine, and mepivacaine. Bupivacaine (n = 20) or mepivacaine (n = 20) was infused into a central vein of anesthetized (isoflurane 1%, Fio(2) 0.21) pigs until mean arterial blood pressure decreased to 50% from baseline. Isoflurane was discontinued and Fio(2) was increased to 1.0. Ten pigs in each local anesthetic group were treated with 20% lipid emulsion (ClinOleic), and 10 pigs with Ringer's solution: 1.5 mL/kg in 1 minute followed by an infusion of 0.25 mL/ kg/min for 29 minutes. Five additional pigs were infused bupivacaine and Intralipid. Total and nonlipid-bound local anesthetic concentrations were determined from repeated blood samples. There were no overall differences in total or nonlipid-bound plasma local anesthetic concentrations between the lipid and Ringer's groups. However, plasma median total bupivacaine concentration was 21% and 23% higher at 20 and 30 minutes, respectively, in the lipid group (P = 0.016 without Holm-Bonferroni correction). There was also no overall difference between lipid and Ringer's groups in the rate of recovery of hemodynamic and electrocardiographic variables. Median mean arterial blood pressure in the lipid group with bupivacaine intoxication was 16 mm Hg and 15 mm Hg higher than in the corresponding Ringer's group at 10 and 15 minutes, respectively (P = 0.016 and P = 0.021, respectively, without Holm-Bonferroni correction). Intralipid also caused no difference between total plasma and nonlipid-bound concentrations of bupivacaine with no apparent enhancement of recovery. Lipid emulsion neither had any measurable effect on the disposition of the studied local anesthetics in plasma, nor did it improve the rate of recovery from intoxication by either local anesthetic as measured by hemodynamic variables./Intralipid/
Litonius ES et al; Anesth Analg 114 (4): 901-6 (2012)
When, in the course of an ageing study, alpha-tocopherol (vitamin E), dissolved in soya oil, was given to 22 Balb/c mice once a week subcutaneously for 10 months, it caused the development of vigorously growing fibrosarcomata at the site of the injections in 17 (77.3%) of the animals. The tumors produced in this manner proved eminently transplantable into syngeneic Balb/c hosts, and have been serially transplanted every 3-4 weeks for over 3 years in such recipients, having reached their 44th transplantation cycle at the present time; upon transplantation, they now exhibit a 100% "take" incidence and proliferate extremely rapidly, growing from pin-head size to up to half the weight of a whole recipient mouse within 3 weeks. All fibrosarcomata showed marked mitotic activity, invasion of adjacent tissues and extensive necrotic areas, and they became more undifferentiated after the third transplantation cycle. Neither pure alpha-tocopherol alone nor soya oil alone produced any tumors when given subcutaneously once a week, for 10 months to groups of 22 Balb/c mice each. It is concluded that the two agents alpha-tocopherol and soya oil which proved non-carcinogenic when injected alone, developed a powerful carcinogenic effect when they acted on subcutaneous connective tissue simultaneously.
Constantinides P, Harkey M; Virchows Arch A Pathol Anat Histopathol 405 (3): 285-97 (1985)
Intralipid (soybean oil), /used/ alone and with heparin during parenteral nutrition, /it/ was investigated in patients and healthy subjects for its effect on lymphocyte and monocyte function. Lymphocyte function in peripheral blood was unaffected, but monocyte function was significantly depressed. Addition of heparin prevented the changes in monocyte function caused by Intralipid, although it had no effect on the immunological parameters by itself. Electron micrographs showed phagocytosis of fat particles by monocytes./Intralipid/
Fraser I et al; JPEN J Parenter Enteral Nutr 8 (4): 381-384 (1984)
Lipid emulsion infusion reverses cardiac toxicity of local anesthetics. The predominant effect is likely creation of a "lipid sink." This in vitro study determined the extent to which Intralipid and Lipofundin sequester anesthetics from serum, and whether it varies with pH. Bupivacaine, ropivacaine, and mepivacaine were added to human drug-free serum (pH 7.4) at 10 ug/mL. The lipid emulsions were added, and the mixture shaken and incubated at 37 °C. Lipid was removed by ultracentrifugation and drug remaining in the serum measured. Additional experiments were performed using 100 ug/mL bupivacaine and at pH 6.9. Lipofundin extracted all three anesthetics to a greater extent than Intralipid (34.7% vs. 22.3% for bupivacaine, 25.8% vs. 16.5% for ropivacaine, and 7.3% vs. 4.7% for mepivacaine). By increasing either concentration of bupivacaine or lipid, there was an increase in drug extraction from serum. Adjusting the pH to 6.9 had no statistically significant effect on the percentage of bupivacaine sequestered. Bupivacaine, ropivacaine, and mepivacaine were sequestered to an extent consistent with their octanol:water partition constants (logP). In contrast with previous studies of extraction of lipids from buffer solutions, an emulsion containing 50% each of medium- and long-chain triglycerides extracted local anesthetics to a greater extent from human serum than one containing exclusively long-chain triglycerides, calling into question recent advanced cardiac life support guidelines for resuscitation from anesthetic toxicity that specify use of a long-chain triglyceride. The current data also do not support recent recommendations to delay administration until pH is normalized./Intalipid/
Ruan W et al; Anesthesiology 116 (2): 334-9 (2012)
For more Interactions (Complete) data for Soybean oil (12 total), please visit the HSDB record page.

11.1.4 Antidote and Emergency Treatment

/SRP:/ Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on the left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Hydrocarbon Blends, Mixtures, and Related Compounds/
Currance, P.L. Clements, B., Bronstein, A.C. (Eds).; Emergency Care For Hazardous Materials Exposure. 3rd revised edition, Elsevier Mosby, St. Louis, MO 2007, p. 247
/SRP:/ Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with 0.9% saline (NS) during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 mL/kg up to 200 mL of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . /Hydrocarbon Blends, Mixtures, and Related Compounds/
Currance, P.L. Clements, B., Bronstein, A.C. (Eds).; Emergency Care For Hazardous Materials Exposure. 3rd revised edition, Elsevier Mosby, St. Louis, MO 2007, p. 247-8
/SRP:/ Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in severe respiratory distress. Positive-pressure ventilation techniques with a bag valve mask device may be beneficial. Consider drug therapy for pulmonary edema ... . Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start IV administration of D5W /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's (LR) if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of pulmonary edema ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Hydrocarbon Blends, Mixtures, and Related Compounds/
Currance, P.L. Clements, B., Bronstein, A.C. (Eds).; Emergency Care For Hazardous Materials Exposure. 3rd revised edition, Elsevier Mosby, St. Louis, MO 2007, p. 248

11.1.5 Human Toxicity Excerpts

/HUMAN EXPOSURE STUDIES/ A double-blind, placebo-controlled, cross-over challenge study of the allergenicity of hydrogenated, partially hydrogenated, and cold-pressed soya bean oils was conducted in a group of seven individuals who had experienced allergic reactions after exposures that had occurred up to 10 years previously. All had positive reactions to a skin-prick test with soya bean extract. The titres of serum immunoglobulin E binding to soya bean proteins were increased in six of the seven patients. None of the subjects reacted to increasing volumes of any of the oils, although the Committee noted that use of gelatin capsules to administer the oils may have masked any reactions of the lips and oral cavity. Although the study provided some evidence that the oil used was not allergenic, appropriate descriptions of the manufacturing process and the consequent specifications of the oil were not provided, and the results could not be extrapolated to other oils.
WHO; WHO Food Additives Series: 44; Potential Allergenicity of Refined Food Products Peanut Oils and Soya Bean Oils (2000); Available from, as of June 26, 2014: https://www.inchem.org/documents/jecfa/jecmono/v44jec11.htm
/HUMAN EXPOSURE STUDIES/ The incorporation of lipid emulsions in parenteral diets is a requirement for energy and essential fatty acid supply to critically ill patients. In this study, the toxicity of a lipid emulsion rich (60%) in triacylglycerol of omega-6 polyunsaturated fatty acids on leukocytes from healthy volunteers was investigated. Eleven volunteers were recruited, and blood samples were collected before infusion of a soybean oil emulsion, immediately afterwards, and 18 hours later. The cells were studied immediately after isolation and again after 24 hours or 48 hours in culture. The following determinations were made: composition and concentration of fatty acids in plasma, lymphocytes and neutrophils, lymphocyte proliferation, levels of cell viability, DNA fragmentation, phosphatidylserine externalization, mitochondrial depolarization, reactive oxygen species production, and neutral lipid accumulation. Soybean oil emulsion decreased lymphocyte proliferation and provoked neutrophil and lymphocyte apoptosis and necrosis. Evidence is presented herein that soybean oil emulsion is less toxic to neutrophils than to lymphocytes. The mechanism of cell death induced by this oil emulsion was characterized by mitochondrial membrane depolarization and neutral lipid accumulation but did not alter reactive oxygen species production. Soybean oil emulsion given as a single dose of 500 mL promotes lymphocyte and neutrophil death that may enhance the susceptibility of the patients to infections./Soybean oil emulsion for parenteral diet/
Cury-Boaventura MF et al; J Parenter Enteral Nutr 30 (2): 115-23 (2006)
/HUMAN EXPOSURE STUDIES/ Three men and four women aged 18-63 years who were sensitive to soya beans were recruited into a double-blind placebo-controlled cross-over study of the allergenicity of soya bean oil. The time since the last exposure of the subjects that had resulted in an allergic reaction ranged from < 1 to 10 years. The oils tested were partially hydrogenated, unhydrogenated, and cold-pressed soya bean oils; the placebo was an olive oil. The sequence of administration of the oils during the study was randomized. Before the start of the study, all the subjects reacted to a skin-prick test with soya bean extract, but none gave a positive reaction to a skin-prick test with the test oils. The percent binding of serum IgE antibody to soya bean allergens, assessed in a radioallergosorbent test in six of the seven subjects, was 230-2800% that of a pooled control serum. On the second day of the study, the subjects were challenged with 2, 5, or 8 mL of the assigned oil administered in gelatin capsules, these doses being equivalent to the amount that might be ingested during a meal. Each dose was followed by a 30-min observation period. Challenges to each of the other oils were made after intervals of at least six days. None of the subjects experienced an immediate or delayed adverse reaction, whether typical or atypical of an allergic reaction, to any of the soya bean oils.
WHO; WHO Food Additives Series: 44; Potential Allergenicity of Refined Food Products Peanut Oils and Soya Bean Oils (2000); Available from, as of June 26, 2014; https://www.inchem.org/documents/jecfa/jecmono/v44jec11.htm
/HUMAN EXPOSURE STUDIES/ The effect of soybean oil (Intralipid; I) emulsion on essential fatty acid, lipid and glucose metabolism was studied in 21 preterm infants on parenteral nutrition randomized to receive 0.5 g/kg of intravenous I injection for 5 days (n=10, group A) or 0.5 increased to 2 g/kg/day over 5 days (n=11, group B). Triene/tetraene ratios did not change in group A, but decreased in group B. In both groups, plasma phospholipid linoleate increased, the increase being greater in group B. In both groups, percent content of arachiodonate and 5,8,11-eicosatrienoate decreased and that of oleate remained unchanged. In contrast, absolute content of arachiodonate and oleate tended to increase, and that of 5,8,11-eicosatrienoate remained unchanged. At a I intake of 0.5 g/kg/day, no infants had hyperlipemia. When I intake exceeded one g/kg/day, the frequency of hypertriglyceridemia and free fatty acidemia, with the free fatty acid/molar albumin ratio exceeding 6:1, increased. Plasma glycerol increased slightly, but was substantially less than the rise in enzymatically determined triglycerides. Hyperglycemia was self-limiting and did not require alteration in dextrose intake. It was concluded that (1) infusion of I emulsion at 0.5-2 g/kg/day maintains essential fatty acid status and phospholipid arachiodonate concentrations; (2) significant hyperlipidemia occurs when I intake exceeds one g/kg/day; (3) hyperglycemia associated with I infusion tends to be self-limiting and may not require alteration in lipid or dextrose intake; and (4) enzymatically determined triglycerides may be used to monitor lipid tolerance, provided that allowance is made for a small but systematic overestimation resulting from the rise in plasma glycerol. /Intralipid/
Cooke RJ et al; J Pediatr 111 (5): 767-73 (1987)
For more Human Toxicity Excerpts (Complete) data for Soybean oil (12 total), please visit the HSDB record page.

11.1.6 Non-Human Toxicity Excerpts

/LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ The purpose of this investigation was to study the effects of continuous Intralipid infusions on serum HDL and LDL levels in the rat. Male Fischer 344 rats were infused continuously via central venous catheter with 10% Intralipid for 96 hr and 5, or 2.5% Intralipid for 14 days. Blood samples were collected during the infusion period for total serum cholesterol, HDL-, and LDL-cholesterol measurements. Food intake was monitored during the studies. Total cholesterol, HDL-cholesterol and LDL-cholesterol levels were significantly elevated following 96 hr of infusion with 10% Intralipid with food intake significantly decreased compared to a control group. In a second experiment, animals received a continuous infusion of either 5% Intralipid, 2.5% Intralipid or 0.45% saline for 14 days. Total cholesterol, HDL-cholesterol and LDL-cholesterol were significantly elevated following 14 days of infusion with 5% Intralipid group compared to controls but food intake remained constant for 12 days with no evident toxicity. /Intralipid/
Wasan KM et al; Lab Anim 28 (2): 138-42 (1994)
/LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ Long chain polyunsaturated fatty acids (LC-PUFAs) in the diet reduce risk of cardiac mortality. Fish oils are a dietary source of LC-PUFAs (EPA, DHA) but intake is low in Western diets. Adding beneficial amounts of LC-PUFAs to foods is limited by their instability and potential to impart off-flavors. Stearidonic acid (SDA), a precursor of EPA in man, is more stable than EPA/DHA in food matrices. SDA is present in fish oils (0.5-4%) and in nutraceuticals (echium, borage oil). Genes for Delta6, Delta15 desaturases were introduced into soybeans that convert linoleic and alpha-linolenic acid to SDA (15-30% fatty acids). Since addition of SDA soybean oil into human foods increases SDA intake, toxicology studies were undertaken to assess its safety. In a 28-day pilot study, rats were gavaged with SDA soybean oil at dosages up to 3g/kg body weight/day; no treatment-related adverse effects were observed.//Stearidonic acid (SDA) soybean oil/
Hammond BG et al; Regul Toxicol Pharmacol 52 (3): 311-23 (2008)
/LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ The life-span of stroke-prone spontaneously hypertensive rats (SHRSP) has been reported to become shorter by ingestion of some vegetable oils, including rapeseed oil, when given as the sole dietary fat. The present study was undertaken to examine if the ingestion of rapeseed (canola) oil affects blood coagulating time and erythrocyte membranes. Namely, SHRSP were orally given canola oil or soybean oil as the only dietary fat (10% of diet) for 4 weeks. After the 4-week feeding, activated partial thromboplastin time (APTT) in the canola oil group (19.9+/-0.5 s, N=8) was significantly shorter than that in the soybean oil group (21.6+/-0.6 s, N=8, P<0. 05), though there were no between-group differences in plasma Ca(2+), platelet density and platelet aggregation. Erythrocytes from the canola oil group were less tolerant to low osmotic pressure than those from soybean oil group; the EC(50) values for NaCl concentration to cause hemolysis were 0.42+/-0.004 and 0.40+/-0.005% in the canola oil and the soybean oil groups, respectively (N=10, P<0.01). The canola oil-induced shortening of blood coagulation time and increased fragility in erythrocyte membranes may have relevance to the promotion of strokes in SHRSP.
Naito Y et al; Toxicol Lett 116 (3): 209-15 (2000)
/LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ Poor control of blood pressure leads to hypertension which is a major risk factor for development of cardiovascular disease. The present study aimed to explore possible mechanisms of elevation in blood pressure following consumption of heated vegetable oil. Forty-two male Sprague-Dawley rats were equally divided into six groups: Group I (control)--normal rat chow, Group II--fresh soy oil, Group III--soy oil heated once, Group IV--soy oil heated twice, Group V--soy oil heated five times, Group VI--soy oil heated ten times. Blood pressure was measured at the baseline level and at a monthly interval for six months. Plasma nitric oxide, heme oxygenase and angiotensin-converting enzyme levels were measured prior to treatment, at month-three and month-six later. At the end of treatment, the rats were sacrificed and thoracic aortas were taken for measurement of vascular reactivity. Blood pressure increased significantly (p<0.01) in the repeatedly heated oil groups compared to the control and fresh soy oil groups. Consumption of diet containing repeatedly heated oil resulted higher plasma angiotensin-converting enzyme level and lower nitric oxide content and heme oxygenase concentration. Reheated soy oil groups exhibited attenuated relaxation in response to acetylcholine or sodium nitroprusside, and greater contraction to phenylephrine. As a result of consumption of repeatedly heated soy oil, an elevation in blood pressure was observed which may be due to the quantitative changes in endothelium dependent and independent factors including enzymes directly involved in the regulation of blood pressure. /Heated soy oil/
Leong XF et al; Lipids Health Dis 9:66 (2010)
For more Non-Human Toxicity Excerpts (Complete) data for Soybean oil (15 total), please visit the HSDB record page.

11.1.7 Non-Human Toxicity Values

LD50 rats iv 67.72 (SE, 10.69) mL/kg/Intralipid/
Hiller DB et al; Reg Anesth Pain Med 35 (2): 140-4 (2010)

11.1.8 Protein Binding

Free fatty acids circulate in the plasma, bound to albumin.

11.2 Ecological Information

11.2.1 Environmental Fate / Exposure Summary

Soybean oil's production and use in salad dressings, cooking oils and foodstuffs and in the manufacture of margarine, printing inks, varnishes, paints, soaps, lubricants and biofuels may result in its release to the environment through various waste streams. Soybean oil occurs in the soy pods of soybean plants. If released to air, an extrapolated vapor pressure of 8X10-5 mm Hg at 25 °C indicates the constituent triglycerides of soybean oil will exist in both the vapor and particulate phases in the atmosphere. Vapor-phase soybean oil constituents will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to range from 0.65 to 5 hours. The unsaturated triglycerides will also degrade in vapor-phase by reaction with ozone; the half-life for this reaction in air is estimated to be 0.2 hours. Particulate-phase soybean oil constituents will be removed from the atmosphere by wet and dry deposition. Soybean oil might be susceptible to direct photolysis by sunlight. If released to soil, the constituent triglycerides of soybean oil are expected to have no mobility based upon an estimated Koc of 1X10+10. Some evaporation from soil surfaces may occur based on a slight odor emitted by soybean oil. However, soybean oil is a semi-drying oil that can partially harden, forming a polymeric film, on surfaces exposed to air. It may be susceptible to direct photolysis on soil surfaces exposed to sunlight. Soybean oil is reported to be readily biodegradable, therefore, biodegradation is expected to be an important environmental fate process in soil and water. If released into water, the constituent triglycerides of soybean oil are expected to adsorb to suspended solids and sediment based upon the estimated Koc. The triglycerides in soybean oil are insoluble in water and likely to adsorb strongly to sediment and suspended material; therefore, volatilization from water is not expected to be an important fate process. A reported BCF of <10 suggests the potential for bioconcentration in aquatic organisms is low. Occupational exposure to soybean oil may occur through inhalation and dermal contact with this compound at workplaces where soybean oil is produced or used. Use data indicate that the general population may be exposed to soybean oil via ingestion of foods and food additives containing soybean oil and via dermal contact with this compound or consumer products containing soybean oil. (SRC)

11.2.2 Natural Pollution Sources

The soy pods of soybean plants (Glycine maxima) contain up to four soybeans and the oil content varies between 17-22%(1). Soybean is a member of the Fabaceae family(2,3).
(1) Thomas A; Fats and Fatty Oils. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: June 15, 2001.
(2) USDA; Plants Database. Plant Profile. Glycine max. Available from as of Sept 15, 2014: https://plants.usda.gov/vore/profile?symbol=glma4
(3) Ohio State; Seed ID Workshop. Ohio State Univ, Dept Horticulture and Crop Sciemce. Available from, as of Sept 15, 2014: https://www.oardc.ohio-state.edu/seedid/single.asp?strID=124

11.2.3 Artificial Pollution Sources

Soybean oil's production and use in salad dressings, cooking oils and foodstuffs and in the manufacture of margarine, printing inks, varnishes, paints, soaps, lubricants and biofuels(1,2) may result in its release to the environment through various waste streams(SRC).
(1) O'Neil MJ, ed; The Merck Index. 15th ed., Cambridge, UK: Royal Society of Chemistry, p. 1616 (2013)
(2) Lewis RJ Sr; Hawley's Condensed Chemical Dictionary. 15th ed., New York, NY: John Wiley & Sons, Inc. p. 1166 (2007)

11.2.4 Environmental Fate

TERRESTRIAL FATE: Soybean oil is a triglyceride mixture comprised of fatty acid constituents of linoleic acid (49%), oleic acid (26%), linolenic (11%) and saturated fatty acids (14%)(1). Based on a classification scheme(2), an estimated Koc value of 1X10+10(SRC), determined from a structure estimation method(3), indicates that the constituent triglycerides of soybean oil are expected to be immobile in soil(SRC). Some evaporation from soil surfaces may occur(SRC) based on a slight odor emitted by soybean oil(1). However, soybean oil is a semi-drying oil(4) that can partially harden, forming a polymeric film, on surfaces exposed to air(4,5). Soybean oil is reported to be sensitive to light(6); therefore, it may be susceptible to direct photolysis on soil surfaces exposed to sunlight(SRC). Soybean oil is reported to be readily biodegradable(7), indicating that biodegradation is expected to be an important environmental fate process in soil(SRC).
(1) O'Neil MJ, ed; The Merck Index. 15th ed., Cambridge, UK: Royal Society of Chemistry, pp. 1616 (2013)
(2) Swann RL et al; Res Rev 85: 17-28 (1983)
(3) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of April 29, 2014: https://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
(4) Poth U; Drying Oils and Related Products. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: June 15, 2001.
(5) Funke W et al; Paints and Coatings, 2. Types. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: April 15, 2010.
(6) Hammond EG et al; Soybean Oil. In: Bailey's Industrial Oil and Fat Products, 6th ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf
(7) European Union; Review of Annex IV of the Regulation No. 1907/2006 (REACH), Evaluation of Existing Entries, Appendix 2. Available from, as of April 25, 2014: https://ec.europa.eu/environment/chemicals/reach/pdf/6b_appendix_2.pdf
AQUATIC FATE: Soybean oil is a triglyceride mixture comprised of fatty acid constituents of linoleic acid (49%), oleic acid (26%), linolenic (11%) and saturated fatty acids (14%)(1). Based on a classification scheme(2), an estimated Koc value of 1X10+10(SRC), determined from a structure estimation method(3), indicates that the constituent triglycerides of soybean oil are expected to adsorb to suspended solids and sediment(SRC). The triglycerides in soybean oil are insoluble in water and likely to adsorb strongly to sediment and suspended material; therfore, volatilization from water is not expected to be an important fate process(SRC). Soybean oil is reported to be sensitive to light(4); therefore, it may be susceptible to direct photolysis in water exposed to sunlight(SRC). According to a classification scheme(6), a reported BCF of <10(5) suggests the potential for bioconcentration in aquatic organisms is low(SRC). Soybean oil is reported to be readily biodegradable(5) indicating that biodegradation is expected to be an important environmental fate process in water(SRC).
(1) O'Neil MJ, ed; The Merck Index. 15th ed., Cambridge, UK: Royal Society of Chemistry, pp. 1616 (2013)
(2) Swann RL et al; Res Rev 85: 17-28 (1983)
(3) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of April 29, 2014: https://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
(4) Hammond EG et al; Soybean Oil. In: Bailey's Industrial Oil and Fat Products, 6th ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf
(5) European Union; Review of Annex IV of the Regulation No. 1907/2006 (REACH), Evaluation of Existing Entries, Appendix 2. Available from, as of April 25, 2014: https://ec.europa.eu/environment/chemicals/reach/pdf/6b_appendix_2.pdf
(6) Franke C et al; Chemosphere 29: 1501-14 (1994)
ATMOSPHERIC FATE: Soybean oil is a triglyceride mixture comprised of fatty acid constituents of linoleic acid (49%), oleic acid (26%), linolenic (11%) and saturated fatty acids (14%)(1). According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(2), the constituent triglycerides of soybean oil, which have an extrapolated vapor pressure of 8X10-5 mm Hg at 25 °C(3), are expected to exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase soybean oil triglycerides are degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to range from 0.65 to 5 hours(SRC), calculated from their rate constants of 5.8X10-10 to 7.3X10-11 cu cm/molecule-sec at 25 °C(SRC) that were derived using a structure estimation method(4). The unsaturated triglycerides will also degrade in vapor-phase by reaction with ozone(SRC); the half-life for this reaction in air is estimated to 0.2 hours(SRC), calculated from a rate constant of 1.4X10-15 cu cm/molecule-sec at 25 °C(SRC) that were derived using a structure estimation method(3). Particulate-phase soybean oil may be removed from the air by wet and dry deposition(SRC). Soybean oil is reported to be sensitive to light(5), therefore, it may be susceptible to direct photolysis by sunlight(SRC).
(1) O'Neil MJ, ed; The Merck Index. 15th ed., Cambridge, UK: Royal Society of Chemistry, pp. 11616 (2013)
(2) Bidleman TF; Environ Sci Technol 22: 361-367 (1988)
(3) Yuan E et al; Fuel 84: 943-950 (2005)
(4) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of April 29, 2014: https://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
(5) Hammond EG et al; Soybean Oil. In: Bailey's Industrial Oil and Fat Products, 6th ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf

11.2.5 Environmental Biodegradation

Soybean oil is reported to be readily biodegradable(1).
(1) European Union; Review of Annex IV of the Regulation No. 1907/2006 (REACH), Evaluation of Existing Entries, Appendix 2. Available from, as of April 25, 2014: https://ec.europa.eu/environment/chemicals/reach/pdf/6b_appendix_2.pdf

11.2.6 Environmental Abiotic Degradation

Soybean oil is a triglyceride mixture comprised of fatty acid constituents(1). The rate constant for the vapor-phase reaction of the saturated fatty acid constituents of soybean oil with photochemically-produced hydroxyl radicals has been estimated as 7.3X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(2). This corresponds to an atmospheric half-life of about 5 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(2). The unsaturated constituents are more reactive. The rate constant for the vapor-phase reaction of a typical unsaturated fatty acid constituent mixture of soybean oil with photochemically-produced hydroxyl radicals has been estimated as 5.8X10-10 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(2). This corresponds to an atmospheric half-life of about 0.65 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(2). The unsaturated constituents will also react with atmospheric ozone. The rate constant for the vapor-phase reaction of a typical unsaturated fatty acid constituent mixture of soybean oil with ozone has been estimated as 1.4X10-15 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(2). This corresponds to an atmospheric half-life of about 0.2 hours at an atmospheric concentration of 7X10+11 ozone molecules per cu cm(2). Soybean oil is light sensitive and it can deteriorate with exposed to sunlight(3). However exposure to air and auto-oxidative mechanisms are more important as a degradative process(3). Oil paints consisting of natural drying oils (such as soybean oil) undergo autoxidative polymerization in the presence of atmospheric oxygen and catalytic driers(4); during film formation (curing), atmospheric oxygen reacts with the oil to form hydroperoxides which decompose into radicals and then initiate polymerization(4).
(1) O'Neil MJ, ed; The Merck Index. 15th ed., Cambridge, UK: Royal Society of Chemistry, pp. 1616 (2013)
(2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of April 29, 2014: https://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
(3) Hammond EG et al; Soybean Oil, In: Bailey's Industrial Oil and Fat Products, Sixth Ed, John Wiley & Sons, Inc., pp. 577-653 (2005). Available from, as of April 28, 2014: https://pharosproject.net/uploads/files/cml/1360080729.pdf
(4) Funke W et al; Paints and Coatings, 2. Types. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: April 15, 2010.

11.2.7 Environmental Bioconcentration

Soybean oil has a reported BCF of <10(1). According to a classification scheme(2), these BCF values suggests the potential for bioconcentration in aquatic organisms is low(SRC).
(1) European Union; Review of Annex IV of the Regulation No. 1907/2006 (REACH), Evaluation of Existing Entries, Appendix 2. Available from, as of April 25, 2014: https://ec.europa.eu/environment/chemicals/reach/pdf/6b_appendix_2.pdf
(2) Franke C et al; Chemosphere 29: 1501-14 (1994)

11.2.8 Soil Adsorption / Mobility

Soybean oil is a triglyceride mixture comprised of fatty acid constituents(1). Using a structure estimation method based on molecular connectivity indices(2), the Koc of the constituent triglycerides of soybean oil can be estimated to be on the order of 1.0X10+10(SRC). According to a classification scheme(3), this estimated Koc value suggests that soybean oil is expected to be immobile in soil.
(1) O'Neil MJ, ed; The Merck Index. 15th ed., Cambridge, UK: Royal Society of Chemistry, pp. 1616 (2013)
(2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of April 29, 2014: https://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
(3) Swann RL et al; Res Rev 85: 17-28 (1983)

11.2.9 Volatilization from Water / Soil

Soybean oil is an oil with a slight odor(1) indicating that some evaporation may occur(SRC). Soybean oil is classified as a semi-drying oil(2) which indicates that it can partially harden when exposed to air and is able to form films if modified or mixed with other film-forming components(2). The triglycerides in soybean oil can react with atmospheric oxygen to form polymeric films(2,3). Soybean oil is much slower drying than linseed oil(2). The triglycerides in soybean oil are insoluble in water and likely to adsorb strongly to sediment and suspended material, therfore, volatilization from water is not expected to be an important fate process(SRC).
(1) O'Neil MJ, ed; The Merck Index. 15th ed., Cambridge, UK: Royal Society of Chemistry, pp. 1616 (2013)
(2) Poth U; Drying Oils and Related Products. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: June 15, 2001.
(3) Funke W et al; Paints and Coatings, 2. Types. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: April 15, 2010.

11.2.10 Plant Concentrations

The soy pods of soybean plants (Glycine maxima) contain up to four soybeans and the oil content varies between 17-22%(1).
(1) Thomas A; Fats and Fatty Oils. Ullmann's Encyclopedia of Industrial Chemistry. 7th ed. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: June 15, 2001.

11.2.11 Probable Routes of Human Exposure

According to the 2006 TSCA Inventory Update Reporting data, the number of persons reasonably likely to be exposed in the industrial manufacturing, processing, and use of soybean oil is greater than 1000; the data may be greatly underestimated(1).
(1) US EPA; Inventory Update Reporting (IUR). Non-confidential 2006 IUR Records by Chemical, including Manufacturing, Processing and Use Information. Washington, DC: U.S. Environmental Protection Agency. Available from, as of April 25, 2014: https://cfpub.epa.gov/iursearch/index.cfm
NIOSH (NOES Survey 1981-1983) has statistically estimated that 314,419 workers (142,134 of these were female) were potentially exposed to soybean oil in the US(1). Occupational exposure to soybean oil may occur through inhalation and dermal contact with this compound at workplaces where soybean oil is produced or used. Use data indicate that the general population may be exposed to soybean oil via ingestion of foods and food additives containing soybean oil and via dermal contact with this compound or consumer products containing soybean oil(SRC).
(1) NIOSH; NOES. National Occupational Exposure Survey conducted from 1981-1983. Estimated numbers of employees potentially exposed to specific agents by 2-digit standard industrial classification (SIC). Available from, as of April 29, 2014: https://www.cdc.gov/noes/

12 Literature

12.1 Consolidated References

12.2 NLM Curated PubMed Citations

13 Patents

13.1 FDA Orange Book Patents

14 Interactions and Pathways

14.1 Drug-Drug Interactions

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CONTENTS